Two frequent missense mutations in Pendred syndrome.

Autor: Van Hauwe P; Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Antwerp, Belgium., Everett LA, Coucke P, Scott DA, Kraft ML, Ris-Stalpers C, Bolder C, Otten B, de Vijlder JJ, Dietrich NL, Ramesh A, Srisailapathy SC, Parving A, Cremers CW, Willems PJ, Smith RJ, Green ED, Van Camp G

Publikováno v: Human molecular genetics [Hum Mol Genet] 1998 Jul; Vol. 7 (7), pp. 1099-104.